The Urban Anthropologist as Flâneur; the Symbolic Pattern of Indonesian Cities

Cities are places full of symbols. In the past decades, Indonesian cities have become the cradle of urban symbolism studies. In this article, the author presents the results of these studies. The cities researched differ tremendously, ranging from the national capital to provincial capitals and small towns; some of them, such as Jakarta, are purely colonial in origin, while others are more or less traditional in character. Some of them have a top-down symbolic structure, largely the product of government activities, while others have symbolic configurations which have a more grassroots character and are based in the religious domain. The methodological aspect of urban symbolism fieldwork is explored by the introduction of the concept of flâneur

The summertime plankton community at South Georgia (Southern Ocean): comparing the historical (1926/27) and modern (post 1995) records.

The earliest comprehensive plankton sampling programme in the Southern Ocean was 32 undertaken during the early part of last century by Discovery Investigations to gain a 33 greater scientific understanding of whale stocks and their summer feeding grounds. An 34 initial survey was carried out around South Georgia during December 1926 and January 35 1927 to describe the distribution of plankton during the summer, and to serve as a 36 baseline against which to compare future surveys. We have reanalysed phytoplankton and 37 zooplankton data from this survey and elucidated patterns of community distribution and 38 compared them with our recent understanding of the ecosystem based on contemporary 39 data. Analysis of Discovery data identified five groups of stations with characteristic 40 phytoplankton communities which were almost entirely consistent with the original 41 analysis conducted by Hardy and Gunther (1935). Major groupings were located at the 42 western end of the island and over the northern shelf where Corethron spp. were 43 dominant, and to the south and east where a more diverse flora included high abundances 44 of Nitzschia seriata. Major zooplankton-station groupings were located over the inner 45 shelf which was characterised by a high abundance of Drepanopus forcipatus and in 46 oceanic water >500 m deep that were dominated by Foraminifera, Oithona spp., 47 Ctenocalanus vanus, and Calanoides acutus. Stations along the middle and outer shelf 48 regions to the north and west, were characterised by low overall abundance. There was 49 some evidence that groupings of stations to the north of the island originated in different 50 water masses on either side of the Southern Antarctic Circumpolar Current Front, the 51 major frontal system in the deep ocean close to South Georgia. However, transect lines 52 during 1926/27 did not extend far enough offshore to sample this frontal region 53 3 adequately. Interannual variability of zooplankton abundance was assessed from stations 54 which were sampled repeatedly during 7 recent British Antarctic Survey cruises (1995-55 2005) to the region and following taxonomic harmonization and numerical 56 standardization (ind. m-3), a subset of 45 taxonomic categories of zooplankton (species 57 and higher taxa) from 1926/27, were compared with similar data obtained during the 58 BAS cruises using a linear model. Initially comparisons were restricted to BAS stations 59 that lay within 40 km of Discovery stations although a comparison was also made using 60 all available data. Despite low abundance values in 1926/27, in neither comparison did 61 Discovery data differ significantly from BAS data. Calculation of the percentage 62 similarity index across cruises did not reveal any systematic differences in species 63 composition between 1926/27 and the present. In the light of ocean warming trends, the 64 existence of more subtle changes in species composition is not ruled out, but an absence 65 of finely resolved time-series data make this impossible to determine

Perturbations in Bouncing Cosmological Models

I describe the features and general properties of bouncing models and the evolution of cosmological perturbations on such backgrounds. I will outline possible observational consequences of the existence of a bounce in the primordial Universe and I will make a comparison of these models with standard long inflationary scenarios.Comment: 9 pages, no figure

Observable Dependent Quasi-Equilibrium in Slow Dynamics

We present examples demonstrating that quasi-equilibrium fluctuation-dissipation behavior at short time differences is not a generic feature of systems with slow non-equilibrium dynamics. We analyze in detail the non-equilibrium fluctuation-dissipation ratio X(t,tw) associated with a defect-pair observable in the Glauber-Ising spin chain. It turns out that $X \neq 1$ throughout the short-time regime and in particular X(tw,tw) = 3/4 for $tw \to \infty$. The analysis is extended to observables detecting defects at a finite distance from each other, where similar violations of quasi-equilibrium behaviour are found. We discuss our results in the context of metastable states, which suggests that a violation of short-time quasi-equilibrium behavior could occur in general glassy systems for appropriately chosen observables.Comment: 17 pages, 5 figures; substantially improved version of cond-mat/040571

Life History and Laboratory Rearing of \u3ci\u3eGerris Argenticollis\u3c/i\u3e (Hemiptera: Gerridae) with Descriptions of Immature Stages

The life history of Gerris argenticollis was investigated in Jackson County, Illinois, March-June 1986, and the immature stages were described. The water strider also was reared from egg to adult under laboratory conditions. This univoltine species overwintered as adults that became active in early March, appearing on a temporary woodland pond after the air temperature exceeded 12°C. Seasonal occurrence of the adults and immatures is discussed. Adults were last observed in mid-June. Feeding records are given. G. argenticollis was reared on Drosophila melanogaster adults under a 10L: 14D photoperiod (ca. 2800 lux) at ca. 21°C. The incubation period averaged 12.5 days. The average durations of the five nymphal stadia were 9.0, 7.6, 8.0, 9.2, and 12.0 days. The total developmental period averaged 58.3 days